Label: ALCOHOL PREP PADS- isopropyl alcohol swab

  • NDC Code(s): 63517-600-01, 63517-600-02, 63517-600-50
  • Packager: Cardinal Health 200, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 17, 2023

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  • Active Ingredients

    Isopropyl Alcohol USP, 70% v/v

  • Purpose

    Antiseptic

  • Uses

    For preparation of skin prior to injection

  • Warnings

    For external use only

    Flammable. Keep away from fire or flame

    Do not use

    • with electrocautery procedures
    • in the eyes
    • on mucus membrane
    • on irritated skin

    Stop use and ask doctor if

    • irritation or redness develops
    • if condition persists for more than 72 hours

    Caution

    In case of deep or punctured wounds, consult a doctor

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions for use

    • wipe injection site vigorously and discard
  • Inactive Ingredient

    purified water

  • Principal Display Panel

    CardinalHealth

    NDC 63517-600-01

    REF MW-APM100

    alcohol prep pads

    EN - Medium 70% Isopropyl alcohol prep pad

    FR - Tampon imbibe d'alcool isopropylique a 70%, moyen

    ES - Almohadilla mediana impregnada en alcohol isopropilico al 70%

    CardinalHealth

    X100

    Label

    CardinalHealth

    NDC 63517-600-02

    REF MW-APM

    alcohol prep pads

    EN - Medium 70% Isopropyl alcohol prep pad

    FR - Tampon imbibe d'alcool isopropylique a 70%, moyen

    ES - Almohadilla mediana impregnada en alcohol isopropilico al 70%

    CardinalHealth

    X200

    Label 1

    CardinalHealth

    NDC 63517-600-50

    REF MW-APM50

    alcohol prep pads

    EN - Medium 70% Isopropyl alcohol prep pad

    FR - Tampon imbibe d'alcool isopropylique a 70%, moyen

    ES - Almohadilla mediana impregnada en alcohol isopropilico al 70%

    CardinalHealth

    X50

    Label 2

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PADS 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63517-600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63517-600-5050 in 1 CARTON02/08/2016
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:63517-600-01100 in 1 CARTON02/08/2016
    21 mL in 1 PACKET; Type 0: Not a Combination Product
    3NDC:63517-600-02200 in 1 CARTON02/08/2016
    31 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/08/2016
    Labeler - Cardinal Health 200, Inc. (961027315)
    Registrant - Cardinal Health 200, Inc. (961027315)
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